Helping you reach your audience – wherever they are

Everything by us
and about us

Argos Multilingual 4 min. read
Use This Time Wisely: Seven Proactive Steps to Take Now for EU MDR and IVDR Compliance

Medical device manufacturers (MDMs) have various resources to ensure compliance with the EU Medical Device Regulation (MDR) and In Vitro Diagnostic Regulation (IVDR). Recently, the EU extended these deadlines, giving manufacturers more time for compliance. For instance, conformity assessments for higher-risk devices (class IIb and class III) are now due in 2027, while lower-risk devices […]

Articles
1 9 10 11 12 13 32
Skip to content